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首页> 外文期刊>Economic geology and the bulletin of the Society of Economic Geologists >Physical and Chemical Evolution of the Dabaoshan Porphyry Mo Deposit, South China: Insights from Fluid Inclusions, Cathodoluminescence, and Trace Elements in Quartz
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Physical and Chemical Evolution of the Dabaoshan Porphyry Mo Deposit, South China: Insights from Fluid Inclusions, Cathodoluminescence, and Trace Elements in Quartz

机译:南方达巴斯山斑岩莫矿床的物理和化学演变:石英中流体包裹物,阴离子发光和微量元素的见解

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摘要

The Dabaoshan polynietallie deposits in the Nanling Range, South China, consist of porphyry and skarn-type Mo mineralization genetically related to Jurassic porphyritic intrusions and adjacent strata-bound Cu-Pb-Zn mineralization hosted in mid-Devonian limestone. Porphyry Mo mineralization is characterized by the superposition of multiple generations of crosscutting quartz-bearing veins including: barren quartz veins (VI), quartz-molybdenite veins with K-feldspar alteration halos that host the bulk of the Mo mineralization (V2), quartz-pyrite veins with muscovite alteration (V3), and late base metal mineralization with argillic alteration (V4), as well as limestone-hosted strata-bound Cu-Pb-Zn mineralization (VS). Fluid inclusion petrography and microthermometry combined with cathodoluminescent textures and trace elements in quartz reveal changes in pressure and temperature of the hydrothermal system that formed the deposit.VI and V2 veins are dominated by low-salinity (1-6 wt % NaCl equiv), CO_2-bearing (4-10 mol %) two-phase inclusions with about 35 vol % bubble trapped in the one-phase field above the solvus of the fluid. VI veins are dominated by CL-bright granular quartz mosaics with higher CL intensity than any other vein type. This quartz also contains more Ti than any other vein generation (24-89 ppm), while Al, Ge, and Li concentrations overlap with other vein generations. Molybdenum ore-hosting V2 veins are also dominated by CL-bright granular quartz mosaics, but V2 veins display slightly less CL intensity and correspondingly lower Ti concentrations (10-65 ppm). V3 veins have a broader spatial distribution than VI and V2 veins, extending from inside the porphyries out into the adjacent limestone. These veins are also dominated by low-salinity (2-6 wt % NaCl equiv), CO_2-bearing (4-7 mol %) two-phase inclusions, these containing about 45 vol % bubble trapped above their solvus. V3 veins are dominated by CL-dark quartz with euhedral growth zones of oscillating CL intensity and systematically lower Ti concentrations than previous vein generations (1.5-12 ppm). Minor V4 veins cut all the above vein generations and also occur as late infill in V3 veins. Low-salinity (4-7 wt % NaCl equiv), CO_2-bearing (4-5 mol %) two-phase inclusions with about 20 vol % bubble prevail in V4 veins. V4 veins have the lowest CL-intensity quartz of all vein types, with euhedral growth zones of oscillating CL intensity and the lowest Ti concentration of all vein types (0.54-5.3 ppm).Intersections of fluid inclusion isochores with Ti-in-quartz isopleths indicate that the hydrothermal system evolved from near-magmatic pressures and temperatures of 2.7 ± 0.2 kbars and 650~° ± 40~°C for VI veins to 1.9 ± 0.2 kbars and 530~° ± 40~°C for V2 veins to 0.65 ± 0.2 kbars and 400~° ± 40~°C for V3 veins. V4 veins, which lack rutile, formed as the system cooled to 250~° to 300~°C at maximum pressures of 0.40 to 0.65 kbar.Unlike nearly all other reported porphyry-type ore deposits, quartz-bearing veins from the Dabaoshan porphyry Mo deposit contain few halite-bearing or vapor-dominated fluid inclusions in any vein type. The dearth of such fluid inclusions, coupled with the abundance of two- and three-phase CO_2-bearing low-salinity fluid inclusions in all vein types is evidence that the formation conditions of VI to V4 veins remained above the V-L surface in the H_2O-NaCl-CO_2 system, such that fluid unmixing rarely occurred in the Dabaoshan hydrothermal system. This is further supported by only rare evidence for quartz dissolution textures in all vein types, implying that pressures were dominantly higher than zone of retrograde quartz solubility. Taken together, the fluid inclusions, CL textures, and quartz trace element data indicate that the Dabaoshan poqihyry Mo deposit is one of the deepest formed porphyry-type ore deposits, having formed at depths of 6 to 7 km below surface. The extreme depth and lack of fluid unmixing inhibited Cu precipitation in the
机译:南林南岭的Dabaoshan Polynietalie沉积物包括斑岩和矽卡型钼矿化,与侏罗纪卟啉侵入性和邻近德文郡石灰石中的邻近地层结合的Cu-PB-Zn矿化。斑岩Mo矿化的特征在于多一代横切式轴承静脉叠加,包括:贫瘠石英静脉(VI),石英 - 钼静脉,伴随着莫矿化(V2)的大部分Mo矿化(V2),石英 - 黄铁矿静脉与Muscovite改变(V3)和具有野原改变(V4)的晚基金金属矿化,以及石灰质宿主的地层结合的Cu-Pb-Zn矿化(Vs)。流体包容岩体和微摩体与晶圆和石英中的微量元素结合,揭示了形成沉积物的水热系统的压力和温度变化,vi和v2静脉由低盐度(1-6wt%NaCl等标),CO_2 - 挤出(4-10摩尔%)两相夹杂物,约35体积%的气泡被困在流体溶剂上方的单相区域中。 VI静脉由CL-明亮的粒状石英马赛克主导,CL强度高于任何其他静脉型。该石英还含有比任何其他静脉(24-89ppm)更多的Ti,而Al,Ge和Li浓度与其他静脉几代重叠。钼矿石宿主V2静脉也由CL-亮粒粒状石英马赛克主导,但V2静脉显示略低于CL强度,相应的较低的Ti浓度(10-65ppm)。 V3静脉具有比VI和V2静脉更宽的空间分布,从卟啉内部延伸到邻近的石灰岩内。这些静脉也由低盐度(2-6wt%NaCl Equif),CO_2-轴承(4-7mol%)两相夹杂物支配,这些脉冲夹在其溶剂上方约45体积%的气泡。 V3静脉由Cl-Dark Quartz用Cl-Dark Quartz与Euhedral生长区域为主,振荡Cl强度和系统地降低Ti浓度,而不是先前的静脉世代(1.5-12ppm)。较小的V4静脉切割了所有上述静脉几代,并且在v3静脉中也发生了晚期填充物。低盐度(4-7wt%NaCl Equif),CO_2轴承(4-5摩尔%)两相夹杂物,v4静脉占约20体积泡沫。 v4静脉具有所有静脉类型的最低Cl-强度石英,振荡Cl强度的Euhedral生长区和所有静脉类型的最低Ti浓度(0.54-5.3 ppm)。流体包容性与Ti-in-in-in-in-in-in-inproplethe表明水热系统从近乎岩浆压力和温度的2.7±0.2 kbars的温度和650〜°±40℃的温度达到1.9±0.2 kbars,530〜°±40°C为v2 veins至0.65±0.65° V3静脉为0.2 kbars和400〜°±40°C。 v4静脉,缺乏金红石,随着系统冷却至250〜°至300℃,最大压力为0.40至0.65 kbar.umlike,几乎所有其他报告的斑岩型矿床,石英静脉来自Dabaoshan斑岩莫沉积物含有几个静脉型含量或蒸气束的液体夹杂物。这种流体夹杂物的缺乏,与所有静脉类型的两种和三相CO_2承载的低盐度液体夹杂物相结合,证明VI至V4静脉的形成条件保持在H_2O-中的VL表面上方。 NaCl-Co_2系统,使得德巴山水热系统中的流体解密很少发生。仅通过所有静脉类型的石英溶出纹理的罕见证据进一步支持这一点,这意味着压力均多高于逆行石英溶解度的区域。一起携带流体夹杂物,CL纹理和石英痕量元件数据表明,Dabaoshan Poqihyry Mo沉积物是最深形成的斑岩型矿石沉积物之一,在下面的深度为6至7km。极端深度和缺乏流体,抑制了Cu沉淀

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    State Key Laboratory of Ore Deposit Geochemistry Institute of Geochemistry Chinese Academy of Sciences Guiyang Guizhou 550081 China;

    Department of Geology Western Washington University Bellingham Washington 98225;

    Guangdong Dabaoshan Mining Company Limited Shaoguan Guangdong 512100 China;

    State Key Laboratory of Ore Deposit Geochemistry Institute of Geochemistry Chinese Academy of Sciences Guiyang Guizhou 550081 China;

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